The American Journal of Human Genetics
Volume 62, Issue 3, March 1998, Pages 542-550
Lack of Homozygotes for the Most Frequent Disease Allele in Carbohydrate-Deficient Glycoprotein Syndrome Type 1A
Under an Elsevier user license
open archive
Phosphomannomutase
Transferrin
N-glycosylation
Recessive disease
Nonradioactive-mutation analysis
Jaeken syndrome
Cited by (0)
Copyright © 1998 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.